摘要
Although remarkable progress has been achieved in electrocatalytic water splitting, the design of highly efficient bifunctional catalysts remains a significant challenge, mainly because of the slow kinetics of the oxygen evolution reaction (OER) and the limited stability of non-precious metal catalysts. This work presents a novel heterojunction catalyst consisting of Co–MnO nanocubes anchored on nitrogen-doped graphitic carbon derived from carbonized Ganoderma lucidum mycelium (CGLM), synthesized via an ion-exchange-coupled pyrolysis strategy. The unique fibrous entanglement morphology of CGLM offers ideal anchoring sites for catalytic centers, while preserving its intrinsic three-dimensional porous architecture to establish a continuous conductive network. This structural enhances electron transport efficiency and promotes stable immobilization of Co–MnO nanocubes (Co–MnO -2 /CGLM). Extensive experimental and theoretical investigations demonstrate that the Co–MnO -2 heterogeneous interface induces charge redistribution, synergistically optimizes the hydrogen adsorption free energy (Δ G H = −0.15 eV), and reduces the OER energy barrier, with a rate-determining step of Δ G 4 = 1.69 eV. The catalyst demonstrates remarkable bifunctional activity in alkaline media, exhibiting overpotentials of 105 mV for hydrogen evolution reaction (HER) at 10 mA cm −2 and 250 mV for OER at 50 mA cm −2 . Notably, the assembled electrolytic cell (Co–MnO -2 /CGLM||Co–MnO -2 /CGLM) achieves a voltage of only 1.61 V (50 mA cm −2 ) in overall water-splitting tests and maintains excellent durability, with negligible change in current density during prolonged operation. This study highlights the synergistic effect of heterogeneous structure engineering combined with biomass-derived carbon substrates in reducing reaction barriers and facilitating charge transfer, offering novel perspectives on the design of cost-effective electrocatalysts for sustainable energy conversion.
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